Zonisamide
- Product NDC
- 68071-4152
- 11-digit product format
- 680714152
- Labeler code
- 68071
- Product ID
- 68071-4152_bb62996a-956e-1d43-e053-2995a90a2476
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Zonisamide
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA077651
- Marketing category
- ANDA
- Marketing start
- 2006-01-30
- Marketing end
- 0000-00-00
- Substance
- ZONISAMIDE
- Active strength
- 100 mg/1
- Pharmacologic classes
- Decreased Central Nervous System Disorganized Electrical Activity [PE],Anti-epileptic Agent [EPC],Sulfonamides [CS],Carbonic Anhydrase Inhibitors [MoA],P-Glycoprotein Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68071-4152-3 | 68071415203 | 30 CAPSULE in 1 BOTTLE (68071-4152-3) | 30 capsule | 2017-11-08 | 0000-00-00 | No | No | Current |
| 68071-4152-5 | 68071415205 | 56 CAPSULE in 1 BOTTLE (68071-4152-5) | 56 capsule | 2017-11-08 | 0000-00-00 | No | No | Current |
| 68071-4152-6 | 68071415206 | 60 CAPSULE in 1 BOTTLE (68071-4152-6) | 60 capsule | 2017-11-08 | 0000-00-00 | No | No | Current |
| 68071-4152-9 | 68071415209 | 90 CAPSULE in 1 BOTTLE (68071-4152-9) | 90 capsule | 2017-11-08 | 0000-00-00 | No | No | Current |